Loma salmonae (Putz, Hoffman et Dunbar, 1965) is a common gill parasite of salmonids, and essentially all species in the genus Oncorhynchus are susceptible. Infections occur in both fresh and salt water. Loma salmonae is directly transmissible by ingestion of spores or infected tissue. The parasite infects the wall of blood vessels of various organs, but the gill is the primary site of infection. Initial infection occurs in the intestine, and xenomas are easily detected in the gills by standard histology at 4-6 wk post-exposure. A few presporogonic stages of the parasite are found in the heart endothelium prior to xenoma formation in the gills. Ultrastructure studies of early infections demonstrated that wandering blood cells transport the meronts to the gills, and that merogony occurs in pillar cells and other cells underlying the gill endothelium. Xenomas develop in these cells, resulting in hypertrophied host cells filled with spores. Xenomas ultimately rupture, and are associated with severe inflammation in which free spores are found in macrophages. The parasites are most pathogenic during this phase of the infection, resulting in severe vasculitis and clinical disease. Both rainbow trout (Oncorhynchus mykiss) and Chinook salmon (Oncorhynchus tshawytscha) recover from infections, but free spores persist in kidney and spleen phagocytes for many months after xenomas are absent in Chinook salmon. Fish that have recovered from the infection show strong immunity against the parasite, lasting up to 1 year. Fish are susceptible to infection by other routes of exposure by spores; co-habitation, anal gavage, and intramuscular, intraperitoneal and intravascular injection. Autoinfection probably occurs following release of spores in blood vessels after xenomas rupture. The optimal temperature for L. salmonae infections is 15-17°C, with a permissive range of 11-20°C.
Chronic kidney disease (CKD) leads to profound metabolic and hemodynamic changes, which damage other organs, such as heart and brain. The brain abnormalities and cognitive deficit progress with the severity of the CKD and are mostly expressed among hemodialysis patients. They have great socio-economic impact. In this review, we present the current knowledge of involved mechanisms.
A review of genera within the tribe Lyropaeini is given. Three new genera - Lyrolib gen. n., Horakiella gen. n., and Ambangia gen. n., and a subgenus Macroambangia subgen. n. within Ambangia gen. n. are described. The following twelve new species are proposed as new to science: Ambangia nigra sp. n. (Sulawesi), A. wallacei sp. n. (Sulawesi), Ambangia (Macroambangia) pallidicornis sp. n. (Sulawesi), A. (M.) celebensis sp. n. (Sulawesi), A. (M.) nigricornis sp. n. (Sulawesi), Alyculus wittmeri sp. n. (Sumatra), Horakiella hammondi sp. n. (Malaysia: Sarawak), H. pahangana sp. n. (Peninsular Malaysia), H. emasensis sp. n. (Malaysia: Sabah), Lyrolib minor sp. n. (Sulawesi), L. grandis sp. n. (Sulawesi), and Microlyropaeus dembickyi sp. n. (Sumatra). A key to genera of Lyropaeini is given, and comments on their relationships are provided.
In the present study, we critically revised the recently proposed classification of the subfamily Leishmaniinae Maslov et Lukeš in Jirků et al., 2012. Agreeing with erection of the genus Zelonia Shaw, Camargo et Teixeira in Espinosa et al., 2017 and the subgenus Mundinia Shaw, Camargo et Teixeira in Espinosa et al., 2017 within the genus Leishmania Ross, 1908, we argue that other changes are not well justified. We propose to: (i) raise Paraleishmania Cupolillo, Medina-Acosta, Noyes, Momen et Grimaldi, 2000 to generic rank; (ii) create a new genus Borovskyia gen. n. to accommodate the former Leptomonas barvae Maslov et Lukeš, 2010 as its type and only species; (iii) leave the subfamily Leishmaniinae as originally defined, but establish two infrafamilies within it: Leishmaniatae infrafam. n. and Crithidiatae infrafam. n., Alexei Y. Kostygov, Vyacheslav Yurchenko., and Obsahuje bibliografii
The taxonomy and distribution of rodents in Zambia was comprehensively summarized in 1978 by W.F.H. Ansell in his excellent book Mammals of Zambia. Despite the fact that during the last three decades many new taxonomic revisions of African rodents were published and extensive new material collected, not much work has been done on Zambian rodents since the book publication. Here we summarize the current knowledge of one of the most speciose group of African rodents, the tribe Praomyini, in Zambia. We review available historical records and revise our recently collected material by sequencing the mitochondrial DNA gene of cytochrome b. The presence of eight species of Praomyini in Zambia is documented and the pattern of their geographical distribution is described and discussed. Two species, Praomys minor and Mastomys coucha, are reported for the first time from Zambia and Praomys cf. jacksoni probably represents a new undescribed species. On the other hand, the actual occurrence of Colomys goslingi, known in Zambia only from one historical record, is questionable. The results document the usefulness of the DNA barcoding approach for description of species diversity of taxonomically complicated groups with many cryptic species.
The New World genus Ataeniopsis Petrovitz, 1973 is revised. Fifteen species are recognized including three new species: Ataeniopsis carupanoi sp. n. from Venezuela, A. jaltipani sp. n. from Mexico and A. vinacoensis sp. n. from Argentina. Lectotype of A. haroldi (Steinheil, 1872) is designated, the name of type species A. notabilis Petrovitz, 1973 is reestablished, five species are given in a new combination. The taxa are diagnosed, keyed and illustrated, and biological information and distribution data summarized following the species descriptions. A hypothetical phylogenetic analysis of Ataeniopsis based on cladistic analysis is presented.
Genus-group taxa of Platerodinae are revised and valid taxa are redescribed. The validity of Plateros Bourgeois, 1879 is reinstated. Libnetomimus Kleine, 1927 is made a junior synonym of Libnetis Waterhouse, 1878. Calleros Gorham, 1881, Calloplateros Pic, 1923, Costatoplateros Pic, 1949, Ditoneces Waterhouse, 1879, Libnetomorphus Pic, 1921, Microplateros Pic, 1921, Planeteros Gorham, 1883, Tolianus Pic, 1921, Melampyrus Waterhouse, 1879, and the subgenus Cautirodes Pic, 1921 are considered to be junior synonyms of Plateros Bourgeois, 1879. The subgenus Pseudeuplectus Pic, 1922 is synonymized to Cavoplateros Pic, 1913, and Pseudoplateros Green, 1951 is made a junior synonym of Falsocalleros Pic, 1933. Macrolibnetis Pic, 1938 formerly classified with Platerodini is synonymized to Platerodrilus Pic, 1921. Samoaneros Blair, 1928 is considered to be a junior objective synonym of Melaneros Fairmaire, 1877, which is excluded from Platerodinae and is kept incertae sedis in Lycidae. Fernandum Pic, 1924 and Subdihammatus Kleine, 1926 are transferred to the subfamily Leptolycinae. Teroplas oculatus sp. n. and Microlycus mexicanus sp. n. are described. Neotype of Plateros brasiliensis (Lucas, 1857) and lectotype of Microlycus minutus Pic, 1922 are designated. In order to understand relationships within the subfamily, included genus-group taxa were cladistically analysed.
Species of Rhamnocercinae Monaco, Wood et Mizelle, 1954 are gill parasites of sciaenid fishes (Perciformes). Seven are marine species (three in the western Atlantic and four in oriental Pacific) and one is a neotropical freshwater species (Rio Doce Basin, Brazil). While the status of the subfamily may be questioned, this assemblage of species is apparently supported by several shared apomorphic and plesiomorphic characters, such as: (1) peduncular spines with anterior and posterior roots; (2) haptor laterally expanded, armed with anchors (two pairs); bars (one ventral, two dorsal); 14 hooks and haptoral accessory spines; and (3) double (nested) tubes of the male copulatory organ (MCO), directed posteriorly with the genital pore lying posterior to the MCO. The phylogenetic hypothesis for the eight known species of this clade is: (Spinomatrix penteormos (Rhamnocercoides stichospinus, Rhamnocercoides menticirrhi) Rhamnocercus oliveri (Rhamnocercus rhamnocercus (Rhamnocercus stelliferi, Rhamnocercus bairdiella, Rhamnocercus margaritae)). This hypothesis indicates that Spinomatrix penteormos represents the sister group of all remaining rhamnocercines. The resulting phylogenetic sister-group relationships support the transfer of Rhamnocercus stichospinus Seamster et Wood, 1956 to Rhamnocercoides Luque et Iannacone, 1991 as Rhamnocercoides stichospinus (Seamster et Wood, 1956) n. comb.
Material of Afrotropical Afrocrania Hincks, 1949 (= Pseudocrania Weise, 1892, not Pseudocrania M'Coy, 1851) is revised, and a redescription of the genus is given. This publication is on Afrocrania species in which males have head cavities or extended elytral extrusions. Species without those sexual dimorphic organs will be revised in a subsequent paper. Material of Pseudocrania latifrons Weise, 1892, Pseudocrania foveolata (Karsch, 1882) (= Monolepta africana Jacoby, 1894, = Pseudocrania nigricornis Weise, 1895), and Pseudocrania assimilis Weise, 1903 was examined; Pseudocrania basalis Jacoby, 1907 is excluded from Afrocrania; Afrocrania kaethae sp. n., A. luciae sp. n., A. kakamegaensis sp. n., A. longicornis sp. n., and A. ubatubae sp. n. are newly described species.